Effective Anti-miRNA Oligonucleotides Show High Releasing Rate of MicroRNA from RNA-Induced Silencing Complex

被引:8
作者
Ariyoshi, Jumpei [1 ,2 ]
Matsuyama, Yohei [1 ]
Kobori, Akio [1 ]
Murakami, Akira [5 ]
Sugiyama, Hiroshi [2 ,3 ]
Yamayoshi, Asako [2 ,4 ]
机构
[1] Kyoto Inst Technol, Dept Biomol Engn, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Sci, Dept Chem, Kyoto, Japan
[3] Kyoto Univ, Inst Integrated Cell Mat Sci iCeMS, Kyoto, Japan
[4] Kyoto Univ, Hakubi Ctr Adv Res, Kyoto, Japan
[5] Kyoto Pharmaceut Univ, Dept Clin & Translat Physiol, Kyoto, Japan
关键词
microRNA; RNA-induced silencing complex; anti-miRNA oligonucleotide; TARGET RNAS; IN-VIVO; CANCER; EXPRESSION; INHIBITION; BIOGENESIS; MECHANISMS; REPRESSION; PATHWAYS; MIR-122;
D O I
10.1089/nat.2017.0663
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) regulate gene expression by forming RNA-induced silencing complexes (RISCs) and have been considered as promising therapeutic targets. MiRNA is an essential component of RISC for the modulation of gene expression. Therefore, the release of miRNA from RISC is considered as an effective method for the inhibition of miRNA functions. In our previous study, we reported that anti-miRNA oligonucleotides (AMOs), which are composed of the 2'-O-methyl (2'-OMe) RNA, could induce the release of miRNA from RISC. However, the mechanisms underlying the miRNA-releasing effects of chemically modified AMOs, which are conventionally used as anti-cancer drugs, are still unclear. In this study, we investigated the relationship between the miRNA releasing rate from RISC and the inhibitory effect on RISC activity (IC50) using conventional chemically modified AMOs. We demonstrated that the miRNA-releasing effects of AMOs are directly proportional to the IC50 values, and AMOs, which have an ability to promote the release of miRNA from RISC, can effectively inhibit RISC activity in living cells.
引用
收藏
页码:303 / 308
页数:6
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